Canonical Allele Identifier: PA2499233606
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 998473
ClinVar RCV Id: RCV001294335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Arg1427Ser
CA370911899
NM_000553.6:c.4281G>C
CA370911900
NM_000553.6:c.4281G>T